A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060491



Internal ID18803022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79171946..79205069hg38UCSC Ensembl
Innerchr16:79205843..79238966hg19UCSC Ensembl
Innerchr16:77763344..77796467hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3833124
hg1933124
hg1833124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719075, nssv3559769
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060491
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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